Lista de obras -

A Threat to the Citizen Volunteer?

scientific article published in 1959

A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes ⬇️

artículo científico publicado el 4 de marzo de 2011

A new mutation in GJC2 associated with subclinical leukodystrophy

artículo científico publicado en 2014

Acetylation of C-terminal lysines modulates protein turnover and stability of Connexin-32

artículo científico publicado en 2018

Acute demyelinating neuropathy in a patient with neurolymphomatosis

artículo científico publicado en 2018

Alterations at Arg76 of human connexin 46, a residue associated with cataract formation, cause loss of gap junction formation but preserve hemichannel function

scientific article published on 25 July 2018

Connexin 32 increases the proliferative response of Schwann cells to neuregulin-1 (Nrg1)

artículo científico publicado en 2009

Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct

artículo científico publicado en 2008

Diseases of connexins expressed in myelinating glia

artículo científico publicado en 2017

Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).

scientific article published on 16 June 2013

Functional Requirement for a Highly Conserved Charged Residue at Position 75 in the Gap Junction Protein Connexin 32 ⬇️

artículo científico publicado el 3 de diciembre de 2012

GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems

artículo científico publicado en 2014

Gap junctions couple astrocytes and oligodendrocytes

artículo científico publicado en 2008

Gap junctions in inherited human disorders of the central nervous system ⬇️

artículo científico publicado el 16 de agosto de 2011

Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves

artículo científico publicado en 2014

Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

artículo científico publicado en 2022

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

artículo científico publicado en 2009

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

artículo científico publicado en 2012

Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants

artículo científico publicado en 2008

Increase in chemokines CXCL10 and CCL2 in blood from pigs infected with high compared to low virulence African swine fever virus isolates

artículo científico publicado en 2013

Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations

artículo científico publicado en 2017

Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease

artículo científico publicado en 2007

Normalization of nomenclature for peptide motifs as ligands of modular protein domains

artículo científico publicado en 2002

Pannexin1 is expressed by neurons and glia but does not form functional gap junctions

artículo científico publicado en 2007

Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32

artículo científico publicado en 2003

Patterns of Spontaneous Local Network Activity in Developing Cerebral Cortex: Relationship to Adult Cognitive Function

artículo científico publicado en 2015

Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness.

artículo científico publicado en 2006

Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes.

artículo científico publicado en 2018

Regulatory role of oligodendrocyte gap junctions in inflammatory demyelination

artículo científico publicado en 2018

Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease

artículo científico publicado en 2016

The Legal Basis for Reorganizing Metropolitan Areas in a Free Society

artículo científico publicado en 1962

The MyD116 African swine fever virus homologue interacts with the catalytic subunit of protein phosphatase 1 and activates its phosphatase activity.

artículo científico publicado en 2007

The Rising Challenge to Minority Advance

scientific article published in 1959

The challenge of profound hypoglycorrhachia: two cases of sarcoidosis and review of the literature

artículo científico

Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins.

artículo científico publicado en 2007

Lista de obras de

A Threat to the Citizen Volunteer?

A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes ⬇️

A new mutation in GJC2 associated with subclinical leukodystrophy

Acetylation of C-terminal lysines modulates protein turnover and stability of Connexin-32

Acute demyelinating neuropathy in a patient with neurolymphomatosis

Alterations at Arg76 of human connexin 46, a residue associated with cataract formation, cause loss of gap junction formation but preserve hemichannel function

Connexin 32 increases the proliferative response of Schwann cells to neuregulin-1 (Nrg1)

Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct

Diseases of connexins expressed in myelinating glia

Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).

Functional Requirement for a Highly Conserved Charged Residue at Position 75 in the Gap Junction Protein Connexin 32 ⬇️

GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems

Gap junctions couple astrocytes and oligodendrocytes

Gap junctions in inherited human disorders of the central nervous system ⬇️

Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves

Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants

Increase in chemokines CXCL10 and CCL2 in blood from pigs infected with high compared to low virulence African swine fever virus isolates

Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations

Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease

Normalization of nomenclature for peptide motifs as ligands of modular protein domains

Pannexin1 is expressed by neurons and glia but does not form functional gap junctions

Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32

Patterns of Spontaneous Local Network Activity in Developing Cerebral Cortex: Relationship to Adult Cognitive Function

Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness.

Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes.

Regulatory role of oligodendrocyte gap junctions in inflammatory demyelination

Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease

The Legal Basis for Reorganizing Metropolitan Areas in a Free Society

The MyD116 African swine fever virus homologue interacts with the catalytic subunit of protein phosphatase 1 and activates its phosphatase activity.

The Rising Challenge to Minority Advance

The challenge of profound hypoglycorrhachia: two cases of sarcoidosis and review of the literature

Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins.